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Lumis 150 VPAP ST EUR3 CO

EUDAMED

Class IIa (EU MDR)

Ref 28116

by ResMed PTY LTD

Identity

Trade Name
Lumis 150 VPAP ST EUR3 CO EUDAMED
Device Name
Lumis 100 VPAP S , Lumis 100 VPAP ST , Lumis 150 VPAP ST EUDAMED
Model / Reference
28116 EUDAMED

Identifiers

Primary DI / UDI-DI
00619498281169 EUDAMED
Basic UDI-DI
619498EC1616H EUDAMED
Direct Marketing DI
00619498285099 EUDAMED
EMDN Code
Z1203010504 ADULT AND PAEDIATRIC/NEONATAL PULMONARY VENTILATORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Lumis 150 VPAP ST EUR3 CO by Resmed Pty Ltd — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
ResMed PTY LTD
EUDAMED SRN
AU-MF-000011753
Authorised Representative
ResMed SAS FR-AR-000007151

Sources (1)

  • EUDAMED 05498778-b194-4717-9eef-caf145857bb0 61 fields · synced Jun 19, 2026